• Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    **Associate Director, Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... product at CDMOs + Design and lead method validation and implementation activities for drug substance...validations and implementations. Experience must include time in a GMP environment. + Prior experience overseeing and working with… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Associate Director, IT Regulatory, Clinical,…

    Bristol Myers Squibb (San Diego, CA)
    …Roadmap leveraged and aligned to business outcomes. Drive for value realization. + Lead a group of indirect reports and service providers to deliver effective, ... drives functional direction. **Physical Requirements:** + Standard office environment coupled with GMP production and facility environment. + Must be willing to wear… more
    Bristol Myers Squibb (11/24/25)
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  • Plant Manager

    Altium Packaging (Tracy, CA)
    …Compliance while focusing on value creation with customers and key stakeholders. . Lead problem- solving and process improvement with the plant and customers to ... customer satisfaction on initial shipments. . Audit facility for compliance with GMP standards and maintain plant in compliance with corporate quality requirements.… more
    Altium Packaging (11/24/25)
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  • Sr. Validation Engineer II

    Gilead Sciences, Inc. (La Verne, CA)
    …very limited direct supervision. + Conducts and serves as a lead /coordinator of investigations and corrective and preventative action (CAPA) recommendations related ... or pharmaceutical) required. + Must have in-depth understanding and application of GMP principles, concepts, practices and standards in the US and internationally. +… more
    Gilead Sciences, Inc. (11/22/25)
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  • Doc Control Specialist

    Actalent (Irvine, CA)
    …Ensure QMS compliance with internal standards and external regulatory requirements. + Lead development and modification of QMS processes to align with business ... internal and external audits and support compliance risk assessments. + Promote GMP and GDP principles across the Quality organization. + Collaborate with… more
    Actalent (11/22/25)
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  • Supplier Engineer

    Caldera Medical (Westlake Village, CA)
    …Should-Cost Models for major sub-commodities to support sourcing decisions. * Lead purchase part approval processes. Contribute to risk analysis (PFMEA), validation ... forming. * Experience with quality systems meeting FDA QSR, ISO 13485, MDD, GMP , and GDP requirements. * Proficiency in SolidWorks * Familiarity with operations… more
    Caldera Medical (11/22/25)
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  • Inventory Management Specialist

    Kelly Services (San Diego, CA)
    …and equipment as required -Implement schedule / policies / and group guidelines - Lead projects as required -Flexible to other tasks as priorities shift -Responsible ... customized programs to meet business needs - Knowledge of Good Manufacturing Practices ( GMP ) or Good Practices (GxP) and experience with Inventory Management is a… more
    Kelly Services (11/22/25)
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  • Production Operator

    Niagara Bottling LLC (Stockton, CA)
    …guidelines, rules, and regulations. + Abides by Niagara's Good Manufacturing Practices ( GMP ) and Food Safety Standards at all times. + Maintains general housekeeping ... of Niagara's LIFE competency model, focusing on the following key drivers of success: + Lead Like an Owner + Makes safety the number one priority + Keeps alert for… more
    Niagara Bottling LLC (11/21/25)
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  • Batching Operator

    Niagara Bottling LLC (Stockton, CA)
    …guidelines, rules, and regulations. + Abides by Niagara's Good Manufacturing Practices ( GMP ) and Food Safety Standards at all times. + Maintains general housekeeping ... of Niagara's LIFE competency model, focusing on the following key drivers of success: + Lead Like an Owner + Makes safety the number one priority + Keeps alert for… more
    Niagara Bottling LLC (11/21/25)
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  • Technician I, Manufacturing

    Herbalife (Lake Forest, CA)
    …+ Disassembles, cleans, sanitizes, and reassembles equipment. + Follow established GMP 's, SOP's, electronic batch records. + Ensure equipment logbooks and other ... training sessions. + Other duties as assigned by Supervisor or Lead . **Qualifications** REQUIRED QUALIFICATIONS: Skills: + Good communication skills both written… more
    Herbalife (11/21/25)
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